US 20050109929 A1
A nanodosimeter device (15) for detecting positive ions induced in a sensitive gas volume by a radiation field of primary particle, comprising an ionization chamber (10) for holding the sensitive gas volume to be irradiated by the radiation field of primary particles; an ion counter system connected to the ionization chamber (10) for detecting the positive ions which pass through the aperture opening and arrive at the ion counter (12) at an arrival time; a particle tracking system for position-sensitive detection of the primary particles passing through the sensitive gas volume; and a data acquisition system capable of coordinating the readout of all data signals and of performing data analysis correlating the arrival time of the positive ions detected by the ion counter system relative to the position sensitive data of primary particles detected by the particle tracking system. The invention further includes the use of the nanodosimeter for method of calibrating radiation exposure with damage to a nucleic acid within a sample. A volume of tissue-equivalent gas is radiated with a radiation field to induce positive ions. The resulting positive ions are measured and compared with a determination of presence or extent of damage resulting from irradiating a nucleic acid sample with an equivalent dose of radiation.
50. A nanodosimeter device for detecting positive ions induced in a sensitive gas volume by a radiation field of primary particles, comprising:
an ionization chamber for holding the sensitive gas volume to be irradiated by the radiation field of primary particles, the ionization chamber having an aperture opening;
an ion counter system connected to the ionization chamber for detecting the positive ions, the ion counter system having an ion counter in communication with the aperture opening;
a particle tracking system having a position-sensitive detector for detecting the primary particles passing through the sensitive gas volume; and
a data acquisition system that receives and correlates data from the ion counter system and the particle tracking system.
51. The nanodosimeter of
52. The nanodosimeter of
53. The nanodosimeter of
54. The nanodosimeter of
55. The nanodosimeter of
56. The nanodosimeter of
57. The nanodosimeter of
58. The nanodosimeter of
59. The nanodosimeter of
60. The nanodosimeter of
61. The nanodosimeter of
62. A method for measuring positive ions induced by a radiation field of primary particles, comprising the steps of:
providing a tissue-equivalent gas;
determining a tissue-equivalent sensitive gas volume of the tissue-equivalent gas;
irradiating the sensitive gas volume with the radiation field;
detecting the positive ions induced by the radiation field;
tracking the primary particles that pass through the sensitive gas volume; and
correlating data regarding the positive ions and primary particles.
63. The method of
64. The method of
selecting primary particles using the particle tracking system with a reference energy Eref and a given energy E that pass the sensitive gas volume;
calculating a ratio of N1(Eref) and N1(E), which are the average number of nanodosimeter ion counts for primary particle energies Eref and E, respectively;
using the ratio of N1(Eref) and N1(E) as an approximation for the ratio of dN(Eref) and dN(E); and
computing the differential value w(E) according to the formula
w(E)/w(E ref)=S(E)/S(E ref)N 1(E ref)/N 1(E).
65. A method for calibrating radiation exposure from a first radiation field with the presence or extent of damage to a nucleic acid within a sample, the method comprising the steps of:
providing a tissue-equivalent gas;
determining a tissue-equivalent sensitive gas volume of the tissue-equivalent gas;
irradiating the tissue-equivalent gas and the sample with the first radiation field;
calculating the number of positive ions induced within the sensitive gas volume by the first radiation field;
detecting the presence or extent of damage to the nucleic acid within the sample following irradiation with a second radiation field; and
comparing and correlating the extent of damage to the nucleic acid within the sample with the calculated number of positive ions induced by the first radiation field.
66. The method of
This application claims priority from provisional applications Ser. No. 60/200,533, titled “Nanodosimeter Based on Single Ion Detection,” filed Apr. 27, 2000.
This invention was made with Government support under cooperative agreement number DAMD17-97-2-7016 with the United States Department of the Army. The Government has certain rights in this invention.
According to modern radiobiological concepts, irreversible radiation damage to a living cell is the consequence of multiple ionizations occurring within or near the DNA molecule over a distance of a few nanometers. Such clustered ionization events can lead to multiple molecular damages within close proximity, some of them causing strand breakage and others various base alternations or losses, which are difficult to repair. Unrepaired or misrepaired DNA damages typically lead to cell mutations or cell death.
The measurement of the number and spacing of individual ionizations in DNA-size volumes can be assumed to one of the most relevant for the specification of what can be termed “radiation quality.” By radiation quality, we refer to measurable physical parameters of ionizing radiation that best correlate to the severity of biological effects caused in living organisms. There are a variety of practical applications for such measurements in radiation protection and monitoring, as well as in radiotherapy.
The monitoring and measurement of radiation quality and the investigation of how it relates to the biological effects of ionizing radiation is of prime importance in many different fields including medicine, radiation protection, and manned space flight. For example, heavy charged particles, including protons, carbon ions, and neutrons produce more complex radiation fields than established forms of radiation therapy (protons and electrons). These newer forms of radiation therapy, which are increasingly being used for the treatment of cancer, require a careful study of radiation quality changing with penetration depth in order to avoid unwanted side effects.
The definition of the merits and risks of these new forms of radiotherapy requires a better understanding of the basic interactions these radiations have with DNA. National and international radiation and environmental protection agencies, e.g., the Nation Council on Radiation Protection and Measurements (NCRP) and the International Commission on Radiological Protection (ICRP), are interested in establishing new standards of radiation quality measurements, which are based on individual interactions of radiation with important biomolecules, most importantly, the DNA.
Further, radiation quality measurements are also essential to predict the risks of human space travel. Predictions of the quality and magnitude of space radiation exposure are still subject to large uncertainties. Nanodosimetric measurements of space radiations or simulated ground-based radiations may help to decrease these uncertainties.
The measurement of local ionization clusters in DNA-size volumes requires the development of novel nanodosimetric devices, as these would be most relevant to assess DNA damage. The results of experimental nanodosimetric studies combined with those of direct radiobiological investigations could provide a better understanding of the mechanisms of radiation damage to cells and the reason why some DNA damage is more serious than others leading to cancer or cell death. They would also provide valuable input for biophysical models of cellular radiation damage. There are a variety of practical applications for such measurements in radiation protection and monitoring, as well as in radiotherapy.
Existing methodologies of dosimetry on a microscopic tissue-equivalent scale use microdosimetric gas detectors, for example, tissue-equivalent proportional counters (TEPCs), which measure the integral deposition of charges induced in tissue-equivalent spherical gas volumes of 0.2-10 μm in diameter, i.e., at the level of metaphase chromosomes and cell nuclei. They cannot be used to measure ionizations in volumes simulating the DNA helix. Furthermore, they provide no information about the spacing of individual ionizations at the nanometer level.
The cavity walls of these microdosimetric counters distort the measurements, which is particularly problematic for cavity sizes below the track diameter. It has been suggested to use wall-less single-electron counters to overcome some of these limitations. However, this method is limited by the fairly large diffusion of electrons in the working gas and can only achieve sensitive volume sizes down to the order of ten tissue-equivalent nanometers. The DNA double helix, on the other hand, has a diameter of 2.3 nm.
It has been suggested in the literature to overcome the limitations of microdosimetric counters through the construction of a dosimeter which would combine the principle of a wall-less sensitive volume with the advantage of counting positive ionization ions, which undergo considerably less diffusion than electrons. This would extend classical microdosimetry into the nanometer domain.
This method, called nanodosimetry, is useful for radiobiology based on the premise that short segments of DNA (approximately 50 base pairs or 18 run long) and associated water molecules represent the most relevant surrogate radiobiological targets for study. Instead of measuring the deposition of charges directly in biological targets, nanodosimetry uses a millimeter-size volume filled with a low-density gas at approximately 1 Torr pressure, ideally, of the same atomic composition as the biological medium. Ions induced by ionizing radiation in the working gas are extracted by an electric field through a small aperture and then accelerate towards a single-ion counter. The sensitive volume of the detector is defined by the gas region from which positive radiation-induced ions can be collected using electric-field extraction. This new method would be useful for determining the biological effectiveness of different radiation fields in the terrestrial and extraterrestrial environment.
The problem with prior nanodosimeters, therefore, is that they have lacked means for measurement of the energy and multi-axis position-sensitive detection of primary particles passing through the nanodosimeter, hindering the ability to perform systematic measurements of ionization clusters within a cylindrical tissue-equivalent volume as a function of these important parameters. Further, a method for calibration of a nanodosimeter, e.g., correlating radiation quality with biological damage, has been unavailable. Therefore, the goals of nanodosimetery described above have been a long felt, but as yet unmet need.
It would be desirable, therefore, to have a nanodosimeter which includes a particle tracking and energy measuring system that is capable of multi-axis position-sensitive detection of primary particles passing through the detector within the nanodosimeter, thereby providing the ability to perform systematic measurements of ionization clusters within a cylindrical tissue-equivalent volume as a function of the position of the primary particle and its energy. Once configured with such a particle tracking and energy measuring system, it would be desirable to be able to calibrate the nanodosimeter to correlate the radiobiological data of DNA damage to radiation quality, thereby relating the physics of energy deposition to radiobiological effects.
The present invention meets these needs by providing a nanodosimeter which includes a particle tracking and energy measuring system that is capable of multi-axis position-sensitive detection of primary particles passing through the detector within the nanodosimeter, and of energy measurement of these primary particles. Using the particle tracking and energy measuring system; a method of calibrating the nanodosimeter to correlate the radiobiological data of DNA damage to radiation quality, thereby relating the physics of energy deposition to radiobiological effects, is also provided.
Use of a MWP detector, or preferably a silicon microstrip detector, is provided, as well as a data acquisition system to run such a nanodosimeter, and thereby process primary particles and secondary ionizations on an event-by-event basis. The provided system is able to measure the energy of primary particle, and detect the location of primary particles, and allow on-line reduction of very large statistical samples, capable of simultaneous detection and counting of particles
The apparatus and method measure individual ions produced by ionizing particles in a wall-less, low-pressure gas volume, which simulates a biological sample of nanometer dimensions. Changing pressure conditions, the size of the sensitive volume can be modified. Modifying the electrical field configuration inside the detector, also the shape of the sensitive volume can be adjusted. The detector registers the number of ions produced in the sensitive volume as well as their spacing along the principal axis of the sensitive volume; both quantities are believed to be important for the biological effectiveness of terrestrial and extraterrestrial radiation. The new detector can be used to provide input data of biophysical models that can predict the biological efficiency or quality of the radiation under investigation. Another novel aspect of the device is that almost any gas composition can be used in order to study radiation effects in the various subcompartments of the biological system, e.g., water and DNA.
These and other features, aspects, and advantages of the present invention will become better understood with reference to the following description, appended claims, and accompanying drawings, where:
The present invention will be better understood with respect to
Various cellular subsystems, most importantly water and DNA, can be simulated by using gases of different composition. As standard gas, one may use propane. As the low-energy ions do not undergo gas multiplication there are no limits on the gas 23 to be investigated.
Individual ions collected from the sensitive volume are counted with a vacuum-operated electron multiplier 12 of a type usually employed in mass spectroscopy. The model 14180HIG active film multiplier, SGE, or an equivalent, would be suitable. The counter generates fast signals from multiplied secondary electrons originating from the interaction of the accelerated ions with the multiplier cathode.
The ion counter 12 requires a vacuum in the order of 10−5 Torr. Maintaining this vacuum against the pressure of about 1 Torr in the ionization chamber 10 requires use of a differential pumping system consisting of two powerful turbo-molecular pumps. Pumps suitable for the purpose include the Varian Vacuum Technologies, Inc., models V250 for pump 14, and model V550 for pump 13, as shown in
A primary particle detection system which provides identification of single particle events must be added to the nanodosimeter 15. Furthermore, this provides for the measurement of the arrival time of the ions relative to the primary particle passage, thereby enabling the spatial localization of the ionization event along the principle symmetry axis of the sensitive volume. Due to the low mobility of the ions, the events are well separated in time. It has been shown that a spatial resolution of 1 nm tissue equivalent length can be achieved.
In this embodiment, the data acquisition process can also be synchronized to gate signals provided by the external radiation source, for example, a synchrotron which delivers particles in form of spills with a complex time structure.
Very large statistical samples must be accumulated with the nanodosimeter to detect rare high-order ionization events. Readout schemes for on-line reduction of such samples, utilizing a digital signal processor located on front-end boards 84 and 85 and embedded computer networks 83, as shown in
In this embodiment, the front silicon-strip detector module comprises two single-sided silicon micro-strip detectors with orthogonal strip orientation, and the back detecor module comprises one double-sided silicon micro-strip detector located behind the sensitive volume. This arrangement of detectors provides information about the primary particle track from the strip-hit information as well as the particle's energy over a wide range of energies. This allows quantifying the nanodosimeter information as a function of the primary particle energy and position.
For the readout of the fast silicon detector signals, it is preferable to use a low-noise, low-power front end ASIC, such as was developed for the GLAST mission, in which the input charge is measured through the pulse width, i.e., as a time-over-threshold (TOT) signal, over a large dynamic range. An example of the measured electronic calibration of the chip TOT vs. input charge (in units of charge deposited by a minimum ionizing particles, MIP) is shown in
Monte Carlo calculations with low energy proton beams can be used to test a relationship such as shown in
Each of the described embodiments for a position-sensitive tracking system requires a data acquisition system (DAQ), that receives input from the ion counter 12, primary particle trigger signals either from the built-in particle tracking system or from scintillators, an accelerator start signal when used with a synchrotron accelerator, and position and energy-deposition data from the particle-tracking system. The DAQ system preferably uses fast PCI technology which receives and sends data from and to an interface board 63 with reference to
In another embodiment, the present invention is a method of correlating the response of the nanodosimeter with the presence or extent of damage to a nucleic acid within a sample. In a preferred embodiment, the nucleic acid containing sample is an in-vitro solution of plasmid DNA. In other embodiments, the DNA is viral, chromosomal, or from a minichromosome.
With reference to
The method further comprises irradiating the tissue-equivalent gas and the sample with a radiation field 121. Preferably, the nucleic acid containing sample is exposed to a substantially equivalent quality of radiation that is measured by the nanodosimeter 15. The plasmid is typically dissolved in an aqueous solution that simulates the cellular environment such as, for example, a solution including glycerol and a buffer. This is done to reproduce the diffusion distance of OH radicals with a living cell. Preferably, the sample is irradiated with a range of doses in order to establish a dose-response relationship. Preferably, the DNA concentration and range of irradiation doses are selected such that each plasmid will, on average, contain about one DNA damage of variable complexity. For example, irradiation of a plasmid sample having a concentration of 1 mg/ml with a dose of about 10 Gy of low-LET radiation will result, on average, in one single stranded break for each plasmid.
In a preferred embodiment, the number of positive ions induced within the tissue-equivalent sensitive volume by the radiation field is detected 122 using an embodiment of the nanodosimeter with particle tracking and energy measuring system described herein.
The frequency distribution of damages of variable complexity to the nucleic acid within the sample is compared with the frequency distribution of variable clusters of positive ions induced within the tissue-equivalent sensitive volume. By damage of variable complexity we refer to base damages (B) or strand breaks (S) occurring on either strand of the DNA and ranging from a single damage site to multiple combinations of these damages.
One embodiment of the calibration assay is illustrated in
The different physical states of plasmids (supercoiled, open circle, linear) are separated by agarose gel electrophoresis and quantified after staining with a fluorescent dye 123. The calibration assay allows one to distinguish and to measure 125 the absolute or relative frequency of the following types of DNA lesions: lesions that contain at least one strand break on one strand but not on the other strand (S0); lesions that contain at least one base damage on one strand but not on the other strand (B0); lesions that contain at least one strand break on complementary strands (SS); lesions that contain at least one base damage on complementary strands (BB); and lesions that contain at least one base damage on one strand and at least one strand break on the other strand (SB).
According to another embodiment of the calibration assay shown in
In this way, one can measure the fraction of unrepaired or misrepaired damage in a given amount of DNA for different radiation qualities, and by comparison with nanodosimetric event spectra 128, identify ionization events leading to mis-reparable DNA damage.
In another aspect of the invention, the probability that a single ionization event proximal to a nucleic acid will result in a single strand break or a base damage is determined by the calibration assay. From this, the frequency of the each type of nucleic acid lesion is calculated for ionization clusters of a given size. The calculated frequency of particular nucleic acid lesions for ionization clusters of a discrete size is compared with the frequency distribution of ionization clusters measured with the nanodosimeter to predict the absolute and relative frequency of each type of nucleic acid lesion.
Although the present invention has been described in considerable detail with reference to certain preferred versions thereof, other versions are possible. For example, in alternative embodiments the invention includes a method for determining a dose of radiation for radiation therapy using the procedure, a method of predicting death or mutation in a living cell, a method of modeling the effect of radiation in a living cell, a method evaluating radiation risk for manned space missions, and assessment of radiation exposure of aircraft crew and frequent flyers. The present invention has many potential applications to various areas including but not limited to planning and optimizing of radiation therapy with charged particles, design and evaluation of radiation shielding, radiation protection, monitoring of occupational and other terrestrial radiation environments. Therefore, the scope of the appended claims should not be limited to the description of the preferred versions described herein.
One particularly important and novel application of the nanodosimeter is the determination of W, the average energy required to produce an ion pair in gases as a function of particle energy. More accurately, W is the quotient of E and N, where N is the mean number of ion pairs formed when the initial kinetic energy, E, of a charged particle is completely dissipated in the gas. While W is known with good accuracy only for a limited number of particle types and energies, accurate knowledge of the energy dependence of W is highly desirable both for basic understanding of dosimetric theory and for application in medical dosimetry. For example, accurate determination of the dose delivered in neutron or proton therapy requires mapping of the energy dependence of W for protons and heavy recoil ions over a wide range of energies with an accuracy of better than 2%. This goal has currently not been accomplished.
The nanodosimeter can be used to measure the differential value, w(E), of the mean energy necessary to produce an ion pair relative to a known value W(Eref) at a reference energy Eref. The differential value w is defined as the quotient of dE by dN, where dE is the mean energy lost by a charged particle of energy E traversing a thin gas layer of thickness dx, and dN is the mean number of ion pairs formed when dE is dissipated in the gas. Alternatively, one may express w as a function of the stopping power S(E)=dE/dx of the gas, which is usually known with good accuracy:
With the particle tracking system of the nanodosimeter one can select primary particles with the reference energy Eref and a given energy E that pass the sensitive volume of the nanodosimeter at a given distance y from the aperture. The ratio of N1(Eref) and N1(E), the average number of nanodosimetric ion counts for primary particle energies Eref and E, can then be used as a good approximation for the ratio of dN(Eref) and dN(E), thus
All features disclosed in the specification, including the claims, abstracts, and drawings, and all the steps in any method or process disclosed, may be combined in any combination, except combinations where at least some of such features and/or steps are mutually exclusive. Each feature disclosed in the specification, including the claims, abstract, and drawings, can be replaced by alternative features serving the same, equivalent or similar purpose, unless expressly stated otherwise. Thus, unless expressly stated otherwise, each feature disclosed is one example only of a generic series of equivalent or similar features.
Any element in a claim that does not explicitly state “means” for performing a specified function or “step” for performing a specified function, should not be interpreted as a “means” or “step” clause as specified in 35 U.S.C. § 112.
Although the present invention has been discussed in considerable detail with reference to certain preferred embodiments, other embodiments are possible. Therefore, the scope of the appended claims should not be limited to the description of preferred embodiments contained in this disclosure.